Main purpose of the job :
- To recruit, screen and provide clinical management to participants in clinical trials according to study protocols
Location :
Wits RHI -7 Esselen Street, Hillbrow, Research Centre. On the 3rd,4th, and 5th FloorKey performance areas :
Clinical assessment, treatment and / or referral of participants who participate in the studyParticipate in routine assessment of participants in accordance with the protocolsInitiate, maintain and strengthen referral systems via direct interaction and assist in the establishment of Memorandums of understanding (MOUs) as required by the study protocol / sConduct regular liaison with the laboratory regarding the interpretation of diagnostic test results. It is the responsibility of the clinician to ensure that an appropriate management plan is followed as a result of receiving diagnostic test resultsManagement of Hepatitis B vaccinations of Research Centre Staff and maintain accurate recordsScreen and enrol eligible patients in accordance with study protocol and ethical guidelinesDemonstrate cultural competence and the ability to work respectfully and effectively with LGBTQIA+ and Gender-diverse populationsReview patient vitals and other study-related resultsTreat opportunistic infections diagnosedPrescribe the appropriate treatmentReport any adverse events and follow-up on patientsConduct regular emergency trolley inventory, order / replace expired consumablesProvide regular clinical support to the clinic staff to ensure that clinical management of participants is of a high quality and complies with HPCSA and WITS RHI standardsData collection and storage of data according to GCP and study SOPâsRecruitment and retention according to set accrual targets as required by the sponsorsDevelopment and ongoing revision of standard operating procedures compliant with sponsor and unit guidelinesIdentify research questions in specialist areaWrite grant proposals, protocols and ethics applications to fund and perform research studiesImplement research studies in conjunction with the research teamsAttend, present and participate in organisational research and academic meetingsProduce monthly progress reports which document clinical outcomes of study participantsComplete source notes and patient logsCapture patient data on the Case Report Forms (CRF)Attend meetings as requiredEngage and meet with Sponsors and Monitors as requiredAttend to all staffing requirements and administrationSupervise and manage the duties of subordinates to ensure optimal staff utilisation and maintenance of sound labour relationsPerform and facilitate performance development and assessmentsIdentify substandard performance by team members and take necessary corrective actionCoach and train subordinates and team members to ensure the acquisition of knowledge and skills required by the organisationPromote harmony, teamwork and sharing of informationTake ownership and accountability for tasks and demonstrate effective self-managementFollow through to ensure that quality and productivity standards of own work are consistently and accurately maintainedMaintain a positive attitude and respond openly to feedbackTake ownership for driving own career development by participating in ongoing training and development activities such as workshops, forums, conferences etc.Participate and give input in ad hoc projects and initiativesComply with Good Clinical Practice (GCP), Protocol requirements and Standard Operating Procedures (SOPs)Verify accuracy of data in source documentation and accuracy of transcription from source data Case Report Forms (CRF) as neededUse Electronic Data Capture (EDC) systems in real-time capture collected dataEnsure errors on source documents e.g. CRFâs are corrected, initialled and datedEnsure completion of corrective action of internal and external QC reports and monitoring reviewsAssist with staff training (and retraining) where error trends are identifiedProactively resolve protocol queries and missing data with the Research TeamRequired minimum education and training :
MBBCh Degree or EquivalentProfessional Body Registration :
Health Professions Council of South Africa (HPCSA)Required minimum work experience :
Minimum 3 years of experience of which 1 year should be in a research environmentDesirable additional education, work experience and personal abilities :
Experience working in a donor funded organizationPost graduate qualification in Public Health / HIV management or in the process of obtaining qualificationExperience in Reproductive HealthExperience in writing donor proposals, protocols and scientific journalsCertification in HIV Management and Good Clinical Practice (GCP)Well organized, ordered, systematic and analyticalWorking knowledge of Microsoft OfficeAssertive, confident and adaptableAble to work under pressure and adhere to deadlinesSelf-motivated, able to work independently and work as part of a multidisciplinary teamDisplay a concern for patients and willingness to respond to patientsâ needs and requirementsAble to priorities own workload, take initiative (proactive) and work to tight deadlinesSelf-motivated with a high regard for work ethic, values and integrityDemands of the job :
National and international travel and overtime may be required from time to time required to be contactable at all times, when at workWorking in under-resourced and / or unpleasant circumstancesMay be required to conduct clinical trial rounds to visit patients if admitted to hospitalWork with participants from all walks of life, all ages including those who are HIV positive, ill and emotional because of the HIV diseaseConfidentiality, tact and discretion must be always maintainedTO APPLY :
Only if you meet the minimum job requirements and experience as mentioned above, you may submit a detailed updated CVPlease Apply Online and complete your registration via our website to enable and protect you as a candidate, and to accept the new POPIA terms and conditionsThis will then create your permanent profile with which you can apply for all jobs as advertised by AJ PERSONNELHowever, you may remove your profile from AJ PERSONNEL when you are no longer in the job marketPlease take note that the applicants who do not adhere to the above criteria will not be considered for the respective positionWits Health Consortium will only respond to shortlisted candidatesCandidates who have not been contacted within two weeks of the closing date can consider their applications to be unsuccessfulClosing date : 24 July 2025Note : No CV will be accepted after the closing datePlease note :
WHC, in accordance with its Employment Equity goals and plan, will give preference to suitable applicants from designated groups as defined in the Employment Equity Act 55 of 1998 and subsequent amendments theretoAJ Personnel is only responsible for advertising and the response handling on behalf of their client Wits Health ConsortiumAJ Personnel does not have any salary or other information regarding the position